| HS Code | 926394 |
| Density | 0.902 g/cm³ |
| Melt Flow Rate | 17 g/10 min (230°C, 2.16 kg) |
| Tensile Strength | 28 MPa |
| Elongation At Break | 50% |
| Flexural Modulus | 1200 MPa |
| Notched Izod Impact | 6 kJ/m² |
| Heat Deflection Temperature | 95°C |
| Melting Point | 163°C |
| Rockwell Hardness | R 90 |
| Water Absorption | 0.03% |
As an accredited MARPOL COPP 17.NB PP Copolymer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | MARPOL COPP 17.NB PP Copolymer is supplied in 25 kg multi-ply paper bags, sealed to protect against moisture and contamination. |
| Container Loading (20′ FCL) | Load MARPOL COPP 17.NB PP Copolymer into 20′ FCL using FIBCs, evenly distributed and secured to prevent shifting. |
| Shipping | MARPOL COPP 17.NB PP Copolymer is shipped as non-hazardous polypropylene granules in moisture-proof woven bags, bulk containers, or railcars. Keep dry, avoid direct sunlight and excessive heat, and store in ventilated areas. Protect packaging from damage during transit to prevent contamination. |
| Storage | Store MARPOL COPP 17.NB PP Copolymer in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep containers tightly sealed to prevent moisture contamination and dust accumulation. Avoid contact with strong oxidizers and acids. Ensure proper labeling and segregation from incompatible materials. No special temperature control required if storage is sheltered from extreme conditions. |
| Shelf Life | Store in a cool, dry place away from sunlight and moisture; shelf life is typically two years from manufacturing date. |
The MARPOL COPP 17.NB PP copolymer grade enters thin-wall food packaging lines as an already nucleated, clarified base resin for dairy cups, lids, and single-serve pots. At a nominal melt mass-flow rate of 17 g/10 min under 230 °C/2.16 kg loading per ISO 1133-1:2022, the material can fill flow-length-to-wall-thickness ratios above 180:1 on sequential valve-gated hot-runner systems without exceeding 120 MPa injection pressure. A converter running 48-cavity stack molds with 0.50 mm to 0.80 mm sidewalls observes that hold pressure above 55 MPa generates gate blush and rim warpage, while mold temperatures below 10 °C increase frozen-in orientation and lid deflection after demolding. For additional haze reduction below 8% at 1 mm thickness measured per ASTM D1003-21, a sorbitol-based clarifier masterbatch is added at 0.10–0.20 wt%. The processing formulation typically includes 0.06–0.12 wt% hindered phenolic/phosphite antioxidant and 0.02–0.05 wt% calcium stearate acid scavenger to limit thermo-oxidative degradation at melt temperatures of 240–250 °C. Food-contact compliance is documented against EU (EU) No 10/2011 as amended, EN 1186-1 overall migration, and FDA 21 CFR 177.1520(c) olefin polymer extraction limits. Terminal packaging includes 125 mL yogurt pots, 500 g margarine tubs, and microwaveable deli containers.
| Process parameter | 0.50–0.80 mm sidewall | 1.00–1.50 mm sidewall |
|---|---|---|
| Melt temperature | 235–250 °C | 220–240 °C |
| Mold temperature | 10–25 °C | 10–30 °C |
| Injection speed | 150–300 mm/s | 60–150 mm/s |
| Hold pressure | 25–50 MPa | 30–55 MPa |
| Back pressure | 4–8 MPa | 4–8 MPa |
| Cooling time | 4–10 s | 12–25 s |
Core shift in cylindrical medical components is driven by differential melt pressure across long unsupported cores. In cleanroom molding with this PP copolymer, a melt temperature of 235 °C and a fill speed below 200 mm/s reduce core deflection, but slow fill increases gate-freeze risk in valve-gated systems. Molds for specimen containers and inhaler actuator bodies use hardened cores above 52 HRC and parting-line interlocks; production-scale failures include black specks from residence time above 260 °C, nucleator plate-out on vent pins, and splay from surface moisture when pellet storage exceeds 60% relative humidity. Pre-drying is set at 80 °C for 2 h with a desiccant dryer dew point of -35 °C when moisture exceeds 0.05 wt%. For biocompatibility, no external mold release agent or slip additive is added; eluate profiles under USP <661.1> and cytotoxicity per ISO 10993-5 are the limiting constraints. Post-mold annealing at 90–100 °C for 20 min relieves molded-in stress but produces 0.5–1.0% additional linear contraction. Published data for this specific grade in ISO 10993-10 configurations is limited; converter-specific extraction and irritation data must be generated for each medical device family. Terminal components include specimen transport containers, inhaler actuator bodies, and centrifuge tube caps.
| Compliance route | Standard / regulation | Test method | Typical acceptance value |
|---|---|---|---|
| EU food contact | EU (EU) No 10/2011 | EN 1186-1 migration cell; food simulants A, B, D2 | Overall migration ≤ 10 mg/dm² or 60 mg/kg |
| US food contact | FDA 21 CFR 177.1520(c) 3.2a | Hexane reflux extraction | Extractables ≤ 5.5% |
| Medical phys-chem | USP <661.1> | Physicochemical panels | Per monograph |
| Medical biocompatibility | ISO 10993-5, ISO 10993-10 | Cytotoxicity, irritation, sensitization | Grade 0 or negative |
| Automotive VOC / fogging | VDA 278, DIN 75201-B | Thermal desorption GC-MS; fogging photometric | TVOC ≤ 100 µg/g; fogging reflectometric ≥ 90% |
For automotive interior compounds, the neat pellet stream from MARPOL COPP 17.NB is compounded on twin-screw extrusion lines with 44:1 to 52:1 L/D ratios and side-feeder positions at the 28 D to 32 D zone for talc addition. A typical 20 wt% talc-filled formulation uses 80 wt% of the clarified copolymer, 20 wt% of compacted talc with median particle size 1.8 µm, 0.15–0.25 wt% hindered phenolic antioxidant, 0.10–0.20 wt% phosphite, 0.10–0.30 wt% HALS UV stabilizer, and 0.02–0.05 wt% calcium stearate acid scavenger. For low-temperature ductility, ethylene-octene POE impact modifier is added at 8–15 wt% depending on the ductile-to-brittle target of the pillar trim. The compounder monitors die melt temperature at 210–230 °C, screw speed 350–550 rpm, and specific mechanical energy input 0.15–0.22 kWh/kg. Production-scale failure modes include vent plugging from fine talc carryover, screw torque excursions when switching from neat PP to 20% talc, and weld-line darkening in door panel bosses. Part designers must account for the higher linear coefficient of thermal expansion of PP relative to ABS or PC/ABS; ISO 11359-2 values for mineral-filled PP copolymer are typically 60–90 × 10-6 K-1, still above PC/ABS at 40–50 × 10-6 K-1. Terminal parts include B-pillar lower trim, glove box bins, and door panel lower inserts where low-gloss and scratch resistance are specified.
Linerless beverage closures molded from this base resin run in 48- to 96-cavity injection-compression tools for 29/25 and 28 mm PCO 1881 shells. The 17 g/10 min flow permits balanced filling without excessive molecular orientation that would otherwise produce anisotropic shrinkage and misaligned knurls. Application torque for a 28 mm PCO 1881 closure typically ranges from 1.5 N·m to 2.5 N·m, while removal torque after hot-fill and ambient cooling must remain below 3.5 N·m on converter-specific torque protocols calibrated to ISO 17025. Organoleptic compatibility with mineral water is assessed via EN 1622 odor panels and in-house taste testing, which limits the choice of peroxide-breakdown antioxidants and external lubricants. Stress-cracking resistance is not reliably evaluated by ASTM D1693-21 for clarified PP copolymer; converters therefore use carbonated bottle retention tests at 2.8–3.0 volumes CO₂ and 38 °C for 72 h to expose microcracks in the tamper-evident bridge roots. Hot-runner temperature is held at 225–240 °C, and mold water is set at 8–12 °C to drive cycle times below 6 s without producing brittle knurl regions. Terminal articles include carbonated soft drink closures, aseptic juice closures, and dairy bottle overcaps.
In clear sheet thermoforming, the 17 g/10 min nucleated PP copolymer is processed through a 90 mm single-screw extruder with a 30:1 L/D two-stage barrier screw and screen pack 100/120/140 mesh. The melt pump must be set to constant discharge pressure 120–180 bar to reduce gauge variation below ±2% across a 600 mm die. The clarified grade improves haze and gloss in sheet, but it requires a controlled calendering stack roll temperature of 60–90 °C to prevent chill-roll bloom from overpowered nucleating additives. Thermoforming downstream uses plug-assisted vacuum forming with aluminum or syntactic foam plugs at sheet surface temperatures of 155–175 °C. Draw ratios above 3:1 require orientation balancing; unsupported cylindrical cup depths above 60 mm may show corner thinning if the sheet is not pre-stretched. Terminal parts include hinged clamshells for bakery goods, clear deli trays with anti-fog coatings, and microwaveable domes under EU (EU) No 10/2011. Production-scale failures include curl from top-to-bottom differential cooling, pinholes from excessive melt temperature above 250 °C, and optical haze drift when regrind addition exceeds 30 wt%.
When small appliance housing converters substitute this PP copolymer for SAN or unreinforced ABS, the first process conflict is not stiffness but differential thermal expansion. ISO 11359-2 linear CLTE for neat PP copolymer is in the 100–150 × 10-6 K-1 range, while SAN is typically 70–80 × 10-6 K-1; the PP part must be designed with wider clearances or ribbed supports to absorb expansion. Mold shrinkage is 1.2–1.8% depending on wall thickness and pigment loading. For load-bearing brackets, 20–30 wt% talc masterbatch is often dry-blended at the machine hopper; this reduces CLTE to 60–80 × 10-6 K-1 but raises melt viscosity. Halogen-free intumescent ammonium polyphosphate packages at 25–35 wt% are used only when the molding temperature is kept below 230 °C because phosphorus-based flame retardants degrade rapidly above this threshold. Production-scale failure modes include sink marks opposite bosses with wall thickness ratio greater than 1.6, color streaks from inadequate mixing in 22:1 L/D general-purpose screws, and cold slug formation when nozzle temperature drops below 210 °C. Terminal components include vacuum cleaner wand cuffs, kettle lower skirts, and iron soleplate shrouds.
In personal-care dispensing packaging, flip-top closures for shampoo and lotion bottles exploit the living hinge behavior of this nucleated PP copolymer only when the gate is located at the hinge-side wall so that flow lines cross the hinge perpendicular to the flex axis. This orientation is confirmed by polarized light microscopy on 0.30–0.35 mm hinge sections. A typical molding formulation includes 0.05–0.12 wt% erucamide slip additive for low closure opening force and 0.10–0.25 wt% glyceryl monostearate antistat where dust pick-up is undesirable. The hinge section is limited to 0.25–0.35 mm; below 0.20 mm, the nucleated copolymer loses tear resistance under high-speed closing, and above 0.40 mm, opening force rises beyond converter limits. Ageing tests at 45 °C and 80% relative humidity for 14 days expose additive bloom, while -20 °C storage can increase opening torque beyond 2.0 N·m by stiffening the hinge. Production-scale deficits include hinge whitening when mold temperature is below 10 °C, center-pin flash on 1.8 mm diameter hinge pins, and stuck hinges from excessive erucamide migration. Terminal articles include two-piece flip-top caps, push-pull closures, and travel bottle overcaps.
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MARPOL COPP 17.NB PP Copolymer is classified as a nucleated polypropylene copolymer for injection molding applications. The numerical designation corresponds to a nominal melt flow rate of 17 g/10 min when measured at 230 °C under 2.16 kg load following ISO 1133-1:2022; if the purchaser’s specification invokes ASTM D1238-23, the values should not be treated as interchangeable without method transfer data. The “NB” suffix is understood as a nucleated base formulation, although the exact nucleating agent chemistry is not disclosed in typical public datasheets and must be confirmed against the certificate of analysis. Lot-specific density is normally reported in the range 0.900–0.910 g/cm³ when measured by ISO 1183-1:2019. Because the grade contains a copolymer fraction, crystallinity and melting enthalpy are lower than those of a homopolymer of equal MFR, which affects stiffness, heat deflection, shrinkage, and low-temperature impact.
The MFR value alone does not define in-mold behavior. When evaluated on a capillary rheometer at 230 °C, a nucleated PP copolymer of this flow class typically exhibits shear viscosity between 20 Pa·s and 60 Pa·s at 1000 s⁻¹. The shear thinning allows filling of ribs, bosses, and long flow paths, but it also narrows the processing window for gate freeze. Melt temperature should be maintained between 220 °C and 250 °C in reciprocating screw injection units. A typical barrel profile from rear to nozzle is 190/210/230/230/230 °C, with screw speed limited to 40–80 min⁻¹ and back pressure below 10 bar unless pigment dispersion requires higher shear. Above 260 °C, unpurged material can undergo thermo-oxidative chain scission, producing surface splay, oxidative degradation odor, and reduced weld-line strength. Below 210 °C, melt elasticity rises and short-shot defects become probable in flow paths with thickness under 0.8 mm when using general-purpose screws with 20:1 to 25:1 L/D ratios. Barrier screws improve plastication uniformity but can lower melt temperature by 3–5 °C at equivalent back pressure because of more efficient melting.
On a production-scale toggle-clamp machine, gate freeze time for a 1.5 mm wall section with a 1.2 mm pin gate is generally 3–5 s. Holding pressure must be maintained until the gate is frozen; premature release produces sink marks and nonuniform shrinkage in areas of molded-in stress. Injection velocity for thin-wall articles is ordinarily profiled between 180 mm/s and 250 mm/s, with holding pressure between 600 bar and 900 bar depending on cavity geometry. These figures are not grade-specific constants; they are equipment-dependent starting conditions that require pilot-tool verification.
The expected property envelope for a medium-flow nucleated PP copolymer class is shown in Table 1 alongside a homopolymer and a lower-flow random copolymer. The data are class-level ranges for comparative positioning and do not replace lot-specific certificate of analysis values.
| Property | Standard | MARPOL COPP 17.NB expected class | PP homopolymer 17 MFR | PP random copolymer 8 MFR |
|---|---|---|---|---|
| Melt flow rate at 230 °C / 2.16 kg | ISO 1133-1:2022 | 17 g/10 min | 17 g/10 min | 8 g/10 min |
| Density | ISO 1183-1:2019 | 0.900–0.910 g/cm³ | 0.900–0.910 g/cm³ | 0.895–0.905 g/cm³ |
| Tensile yield stress at 50 mm/min | ISO 527-2:2012 | 25–27 MPa | 34–36 MPa | 23–25 MPa |
| Flexural modulus | ISO 178:2019 | 1100–1400 MPa | 1500–1800 MPa | 800–1000 MPa |
| Notched Izod impact at 23 °C | ISO 180:2020 | 25–45 kJ/m² | 2–4 kJ/m² | 25–35 kJ/m² |
| Notched Izod impact at -20 °C | ISO 180:2020 | 6–10 kJ/m² | 1.5–2.5 kJ/m² | 2–4 kJ/m² |
| Heat deflection temperature B at 0.45 MPa | ISO 75-2:2020 | 85–100 °C | 105–120 °C | 70–80 °C |
The differences in Table 1 illustrate the structural consequence of the copolymer phase: a flexural modulus penalty relative to homopolymer, an impact advantage at sub-ambient temperature, and lower heat deflection. Against a lower-flow random copolymer, the higher MFR of MARPOL COPP 17.NB reduces fill pressure but sacrifices some optical contact clarity because the heterophasic morphology scatters light.
Mold shrinkage for nucleated PP copolymers in this flow class is typically 1.0–1.6% in the flow direction and 0.8–1.4% transverse when measured on a 60×60×2 mm plaque according to ISO 294-4:2018. Shrinkage anisotropy in heterophasic copolymers arises from orientation of the continuous PP matrix during cavity filling and from differential crystallization around dispersed elastomer domains. For parts with flatness requirements below 0.5 mm TIR, mold design should avoid abrupt wall-thickness steps exceeding 1:1.5 and should place gates in the thickest section to maintain controlled packing. Post-mold cooling fixtures may be needed when ejection temperature exceeds 80 °C. If published tooling shrinkage data for this exact grade is limited, pilot-tool measurement is preferred over estimates taken from homopolymer databases.
When compared with a standard non-nucleated PP impact copolymer of the same nominal MFR, the nucleated variant typically shows a 10–15 °C higher crystallization onset temperature by differential scanning calorimetry at 10 °C/min cooling rate per ISO 11357-7:2022. This shift translates into demolding time reductions of 8–12% in production-scale trials where cooling is the rate-limiting step. However, nucleating agents can increase gate blush and surface gloss sensitivity if injection speed is too high or mold temperature is below 20 °C.
Thin-wall dairy containers, caps, and closures require short filling times at wall thicknesses of 0.5–1.2 mm. In such configurations, the 17 g/10 min MFR allows lower injection pressure than an 8 g/10 min random copolymer, while the copolymer phase retains measurable crack resistance at refrigerator temperatures. The product differs from a homopolymer of equal MFR by lower stiffness and higher impact at low temperature; it differs from a lower-flow random copolymer by longer spiral flow and better heat resistance but lower contact clarity. Published spiral flow length for an equivalent class material is typically 450–650 mm at 2 mm thickness and 700 bar injection pressure. These values should be confirmed on the production tool because geometry, gate size, and machine hydraulic response alter the result.
Automotive interior substrates such as pillar trims and door panel retainers are specification-driven applications. For these parts, tensile strength and flexural modulus may be secondary to notched Izod impact at -20 °C and fogging performance. MARPOL COPP 17.NB falls within the PP copolymer group conventionally screened under ISO 6452:2021 for fogging and VDA 270:2020 for odor where interior VOC limits apply. Long-term heat aging should follow ISO 188:2023 at 110 °C or 120 °C for 500 h intervals; at 120 °C, nucleated copolymers may show more oxidative embrittlement than random copolymers, so continuous service should be limited to 90 °C in air unless antioxidant formulation is verified. Published data for this specific automotive configuration is limited.
Color concentrates and additive masterbatches should use PP-compatible carrier resins. For typical dosing at 2–4 wt%, a PP homopolymer carrier with MFR between 10 g/10 min and 30 g/10 min disperses adequately in single-screw dosing equipment. Peroxide-based vis-breaking masterbatches should be avoided; the nucleated structure is already adjusted for flow, and additional peroxide may shift MFR above 25 g/10 min, reducing impact and increasing gate blush. Amine-based flame retardants or copper inhibitors should be evaluated for antagonism with the nucleating system and acid scavengers. Although polypropylene is not hydrolytically sensitive, storage at relative humidity above 60% can deposit surface moisture; pre-drying in a desiccant dryer at 70–80 °C for 2 h is advisable when surface splay is observed or when vacuum hopper loading is unavailable.
| Requirement | Designation | Documentation to request |
|---|---|---|
| REACH SVHC candidate list | EC 1907/2006 | Article declaration from formulator or distributor |
| RoHS restricted substances | EU 2015/863 | Certificate of conformity |
| Food-contact polypropylene | FDA 21 CFR 177.1520 | Compliance letter if food-contact use is intended |
| EU plastic migration | EU 10/2011 | Overall migration test under OM2 or OM7 |
| Heavy metal content | ISO 11885:2007 or EN 71-3:2019+A1:2021 | Analytical report or heavy-metal certificate |
Where direct food-contact approval is required, the final article must be tested because compliance is not inherent to resin alone and depends on masterbatch, processing aids, mold release, and the thermal history of the molded part.
In reusable crates and logistics totes, the grade can be combined with linear low-density polyethylene regrind at 5 wt% without excessive loss of flexural modulus, but this should be validated using ISO 527-2:2012 and ISO 180:2020 on molded plaques. Blending with post-industrial PP copolymer at 10–15% by weight is a production-level option; however, batch-to-batch variability in ethylene content and nucleant concentration can produce inconsistent shrinkage and Izod results unless each blend lot is tested against the same test methods before release.